Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406058Generated: November 4, 2026

4-chloro-5-nitro-1H-pyrazole-3-carboxylic acid → HCID 178509123, compound

https://huagongshe.com/reaction/2406058

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-chloro-5-nitro-1H-pyrazole-3-carboxylic acidHCID 135420632—
CatalystNickelHCID 935—
CatalystManganeseHCID 23930—
SolventWaterHCID 962—
ProductHCID 178509123HCID 178509123—

Reaction Steps

Crude 16 (10.0 g, 52.2 mmol) was heated in water (100 mL) to 60° C. int. temperature. The product intermediate 16 contained manganese salts as an impurity, but could be used unpurified in the Raney-Ni reduction to obtain intermediate 17. To this solution was added Raney-Ni (7 g, 50% slurry in water) and dropwise over 4 hours a solution of hydrazine monohydrate (20 mL) in water (200 mL). Hydrazine was more effective as a hydrogen source in this reduction than hydrogen provided at 1 bar. After 1 hour at 60° C. int. temperature the mixture was allowed to cool to ambient temperature, filtered through celite, the filter cake washed with water (200 mL) and the combined filtrates evaporated and dried in vacuo to afford crude 17 (15 g, max. 52.2 mmol), which contained some Ni salts and was used unpurified in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809344B2
Source datasetuspto-grants-2014_08
ORD IDord-bdd059015e2e41b1a121799679190e2b
Source noteuspto-grants-2014_08